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Cited by 194

The DOI matches its Crossref record; 20 of the 20 references it cites were found in a registry or an index.

EGFR C797S mutation mediates resistance to third-generation inhibitors in T790M-positive non-small cell lung cancer

Open access
Wang, Shuhang, Tsui, Stella T., Liu, Christina, Song, Yongping, Liu, Delong·2016·Journal of Hematology & Oncology

Abstract

T790M mutation is the most common mechanism for resistance to first- and second-generation tyrosine kinase inhibitors (TKI) for epidermal growth factor receptor (EGFR). Several third-generation EGFR mutant selective TKIs are being explored to conquer this resistance. AZD9291 (osimertinib, tagrisso) has been approved for treatment of the metastatic EGFR T790M mutation-positive non-small cell lung cancer. Resistance to AZD9291 has been described. C797S mutation was reported to be a major mechanism for resistance to T790M-targeting EGFR inhibitors. This review summarizes the latest development in identifying the C797S mutation and EAI045, the novel selective inhibitor overcoming the C797S mutant.

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Metadata

Authors
Wang, S., Tsui, S. T., Liu, C., Song, Y., & Liu, D.
Venue
Journal of Hematology & Oncology
Published
2016-07-22
Volume
9
Issue
1
Pages
59-59
ISSN
1756-8722 (ISSN-L)
OpenAlex
W2490543344
Cited by
194
References
20
FWCI
19.86
Type
journal article
Language
en
Open access
gold

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CoChat. (2026). Citation check: EGFR C797S mutation mediates resistance to third-generation inhibitors in T790M-positive non-small cell lung cancer. https://app.cochat.ai/papers/10.1186/s13045-016-0290-1
The paper
Wang, S., Tsui, S. T., Liu, C., Song, Y., & Liu, D. (2016). EGFR C797S mutation mediates resistance to third-generation inhibitors in T790M-positive non-small cell lung cancer. Journal of Hematology & Oncology. https://doi.org/10.1186/s13045-016-0290-1

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.